Canonical Allele Identifier: PA2825160932
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2935359
ClinVar RCV Id: RCV003791013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Phe173Leu
CA379964795
NM_000378.6:c.519C>G
CA379964796
NM_000378.6:c.519C>A
CA379964804
NM_000378.6:c.517T>C